Doublecortin-like kinase is required for cnidocyte development in Nematostella vectensis

The complex morphology of neurons requires precise control of their microtubule cytoskeleton. This is achieved by microtubule-associated proteins (MAPs) that regulate the assembly and stability of microtubules, and transport of molecules and vesicles along them. While many of these MAPs function in all cells, some are specifically or predominantly involved in regulating microtubules in neurons. Here we use the sea anemone Nematostella vectensis as a model organism to provide new insights into the early evolution of neural microtubule regulation. As a cnidarian, Nematostella belongs to an outgroup to all bilaterians and thus occupies an informative phylogenetic position for reconstructing the evolution of nervous system development. We identified an ortholog of the microtubule-binding protein doublecortin-like kinase (NvDclk1) as a gene that is predominantly expressed in neurons and cnidocytes (stinging cells), two classes of cells belonging to the neural lineage in cnidarians. A transgenic NvDclk1 reporter line revealed an elaborate network of neurite-like processes emerging from cnidocytes in the tentacles and the body column. A transgene expressing NvDclk1 under the control of the NvDclk1 promoter suggests that NvDclk1 localizes to microtubules and therefore likely functions as a microtubule-binding protein. Further, we generated a mutant for NvDclk1 using CRISPR/Cas9 and show that the mutants fail to generate mature cnidocytes. Our results support the hypothesis that the elaboration of programs for microtubule regulation occurred early in the evolution of nervous systems. Supplementary Information The online version contains supplementary material available at 10.1186/s13064-024-00188-0.


Introduction
The elaborate morphology of neural cells is accompanied and enabled by proteins that regulate the assembly and dynamics of the different filaments that constitute the neural cytoskeleton.This can occur via direct stabilization/destabilization of cytoskeletal filaments, their posttranslational modification, or the binding to other molecules and cellular structures [1][2][3][4][5][6].Microtubuleassociated proteins (MAPs), for example, are important for the outgrowth and stability of neurites, for axonal and dendritic transport and for neuronal migration.Some MAPs appear to function specifically in neurons, whereas Doublecortin-like kinase is required for cnidocyte development in Nematostella vectensis others have more generic roles in regulating microtubules in all cells [6][7][8].While neural-specific MAPs have been identified and studied in vertebrates and a few other bilaterians, it is not well understood when during the evolution of nervous systems, they acquired their neural functions.Here we attempt to improve the understanding of the early evolution of neurons by studying the neural microtubule-associated protein Doublecortin-like kinase (Dclk) in the sea anemone Nematostella vectensis.
Doublecortin-like kinases are members of a small family of proteins characterized by the presence of one or two microtubule-binding doublecortin domains [9][10][11].The name of this domain derives from the phenotype caused by mutation of the founding member of this protein family, doublecortin or DCX [12,13].Females heterozygous for mutations of this X-linked gene display a developmental defect of the cerebral cortex called subcortical band heterotopia (also described as double cortex syndrome), whereas males develop lissencephaly, a reduced folding of the cortex [12,13].These phenotypes reflect defects in the lamination of the cortex and are caused by impairment of neural migration required for the correct formation of the cortical cell layers [14,15].In contrast to the situation in humans, mutation of the Dcx gene in mice does not lead to an obvious phenotype in the cortex, though these mice display disorganization of the hippocampus [16].Simultaneous knock-out of mouse Dcx and Dclk1 resulted, however, in neuronal migration and cortical lamination defects resembling those observed in humans carrying DCX mutations [17][18][19].The three mammalian Dclks differ from Dcx by the presence of a C-terminal serine/threonine kinase domain, but these findings suggest that Dcx and Dclk1 have redundant functions in the control of neuronal migration during cortex development in mice.In addition to their role in neuronal migration, Dcx and Dclk1 have been shown to function in the formation of axons and dendrites [17,18,[20][21][22][23].These roles in neuronal migration and neurite formation have been attributed to the ability of Dcx and Dclk1 to bind microtubules, regulate their polymerization and affect the function of other microtubule-binding proteins [10,14,15,20,[23][24][25][26][27][28][29].Dcx and Dclk1/2 have also been shown to interact with actin filaments and this property has been proposed to contribute to the regulation of axon guidance [28,[30][31][32].Outside the nervous system, dcx is expressed in muscle cells [33,34] and Dclk1 has attracted considerable attention as a marker for tumour stem cells in a variety of cancers [35,36].
Outside vertebrates, little is known about the role of Dcx and Dclk genes.A Dcx gene has been identified in the amoebozoan Dictyostelium discoideum, where it has a role in the aggregation of cells during development [37].In Drosophila melanogaster, a gene encoding two dcx domains and multiple C-terminal WD40 domains (DCX-EMAP) is involved in the development and function of mechanosensory cells [38,39], but no specific function has been identified for the Dclk gene CG17528 [40].In Caenorhabditis elegans, the Dclk gene zyg-8 is required for microtubule assembly at the mitotic spindle of zygotes [41] and later during development as a regulator of microtubules mainly in neurons [42].In sea urchin, two Dclk genes are expressed uniformly throughout the embryo [43].Microtubule-binding Dcx domains thus emerged prior to the origin of metazoans, but it remains unclear at which point in evolution Dcx-domain proteins became important for the development of neural cells.
We identified a Dclk gene (NvDclk1) from the sea anemone Nematostella vectensis in a screen for genes whose expression is altered in conditions of increased or decreased neurogenesis (G.Richards, J. Blommaert, F. Rentzsch, unpublished data).Nematostella belongs to the cnidarians (e.g.corals, jellyfish, sea anemones) which are the sister group to the bilaterians (e.g.vertebrates, arthropods, nematodes) with a divergence time > 600 million years ago [44][45][46].Cnidarian polyps are sessile, tube-shaped animals with a single body opening that is surrounded by tentacles for the capture of prey.Due to simple culture conditions and a relatively well-developed suite of tools for genetic manipulations, Nematostella vectensis has emerged as an important cnidarian model organism [47,48].Development in Nematostella includes a hollow blastula stage, gastrulation by invagination and a free-swimming planula stage before the animals transform into sessile and feeding primary polyps [47,49,50].Neurogenesis occurs throughout the body column in tissues derived from both ectoderm and endoderm (the only two germ layers in cnidarians).It commences at blastula stage with the appearance of progenitor cells that give rise to secretory cells and the main classes of cnidarian neural cells, i.e. sensory/sensory-motor neurons, ganglion neurons (morphologically resembling interneurons) and the cnidarian-specific cnidocytes (stinging cells) [51][52][53][54][55][56].The genetic programs controlling neurogenesis in Nematostella and in diverse bilaterians share many signalling molecules and transcription factors [48,[57][58][59][60][61][62][63], but how molecules involved in the elaboration of neuronal morphology and subcellular structures compare between cnidarians and bilaterians, is not well understood.
Using expression analyses and transgenic reporter lines, we show here that NvDclk1 is expressed in neurons and cnidocytes and that the NvDclk1 protein is associated with microtubules in cnidocytes.The transgenic lines reveal a dense network of neurite-like processes emerging from cnidocytes in the tentacles.We also generated a NvDclk1 mutant line via CRISPR/Cas9 and found that these mutants display defects in the development of the extrusive capsule of the cnidocytes.These observations support the hypothesis that regulation of microtubules by doublecortin-domain proteins is an ancient feature of nervous system development.

NvDclk1 is expressed in scattered cells from blastula stage on
We identified two doublecortin-like kinase genes in the Nematostella genome, which we termed NvDclk1 and NvDclk2.Both contain two dcx domains, typical of the Dclk1/2 subgroup and different from most Dclk3s that possess only one dcx domain [9,64].Two additional predicted genes encoding two N-terminal dcx domain, but no kinase domain, were most similar to vertebrate Dcdc2 genes in BLAST searches (Fig. 1A [9,11]) .For NvDclk1, we cloned two splice variants, one encoding the dcx and kinase domains (NvDclk1-long or NvDclk1l); and one that lacks the kinase domain (NvDclk-short or NvDclk1s, Fig. 1A).NvDclk1s is not a truncated version of NvD-clk1l, instead the entire sequence after the second dcx domain is derived from exons that are not present in the mature NvDclk1l transcripts (Fig. 1A).Using a probe that recognizes both splice variants, we found that NvDclk1 is first detectable at mid-blastula stage in a patch of tissue (Fig. 1B).At late blastula stage, this tissue thickens, identifying it as the future oral region that will give rise to the endoderm (Fig. 1C [49,50]) .In addition, expression becomes visible in individual cells distributed throughout the blastoderm (Fig. 1C).The number of these cells increases during gastrulation, whereas the expression in the invaginating endoderm ceases (Fig. 1D, E).During planula stages, expression of NvDclk1 remains detectable in the scattered ectodermal and endodermal cells of the body column and in particular around the oral pole, the site where the tentacles with a high density of cnidocytes form (Fig. 1F, G).NvDclk2 is expressed throughout the Nematostella tissue, with higher levels in the pharynx during planula stages (Fig. 1H-J).Since the expression pattern of NvDclk1 resembles the distribution of neural cells, we focused our subsequent analyses on this gene.

A NvDclk1::GFP reporter line labels cnidocytes and neurons
To gain better insight into a potential expression of NvDclk1 in neural cells, we first analysed existing transcriptome data.NvDclk1 transcripts are enriched in transcriptomes derived from NvElav1::mOrange + neurons (3.4 fold) and from NvNCol3::mOrange2 + cnidocytes (2.1 fold), both generated at primary polyp stage [61,63,65,66].Next, we generated a transgenic reporter line in which a 2.9 kb genomic DNA fragment immediately upstream of the NvDclk1 start codon drives the expression of a membrane-tethered green fluorescent protein (GFP).We used double fluorescence in situ hybridization (DFISH) in this NvDclk1::GFP transgenic line to assess how well the line represents NvDclk1 expression.Nearly all GFP expressing cells were also expressing NvD-clk1 (97.5 ± 0.6% at gastrula, 97.9 ± 3.6% at planula stage, n = 3 for each stage), but we also observed many NvDclk1 expressing cells that did not express GFP (32.4 ± 5% of all NvDclk1-expressing cells at gastrula, 42 ± 17.4% at planula stage, Fig. 2A-F).The transgenic line can thus be used for tracing NvDclk1-expressing cells, though it does not identify all of these cells and their progeny.GFP-positive cells were detectable from gastrula stage on (Fig. 2G) and remained visible throughout the body column at planula and tentacle bud stages (Fig. 2H-K).From mid-planula stage on, strong GFP signal was visible at the oral end, in the developing tentacles (Fig. 2I-K).While the signal in the tentacles was readily visible in animals derived from crosses of NvDclk1::GFP and wildtype animals, the signal in the body column was clearly visible only in a fraction of planulae and polyps derived from incrosses of NvDclk1::GFP animals.We assume that animals with visible signal in the body column contain two alleles of the transgene.Notably, we did not observe GFP expression in the pre-endodermal plate and the invaginating endoderm, despite clear signal in the NvDclk1 in situ hybridizations.
To test whether NvDclk1::GFP labels cnidocytes, we labelled cnidocysts (the extrusive capsule inside cnidocytes) with an antibody against the minicollagen NvN-Col3 [67].Both at gastrula and planula stages, many of the GFP-positive cells also stained for NvNCol3 (Fig. 3A,  B).At gastrula stage, many of the NvNCol3 -labelled cnidocysts were small (Fig. 3A), suggesting that the transgene identifies cnidocytes at an early stage in their development.At planula stage, NvDclk1::GFP-positive cnidocytes were visible both in the pharynx and in the tentacle buds (Fig. 3B).Crossing the NvDclk1::GFP animals to a NvNCol3::mOrange2 line [65] showed that many of the labelled cnidocytes possess multiple long processes with bifurcations and varicosities, morphologically resembling neurites (Fig. 3C, D), as also described by Karabulut et al., 2022 [68] and partially visible in Weir et al., 2020 [69].This network of cell processes was visible both in the tentacles and in the body column.
Observation of polyps mosaic for the NvDclk1::GFP transgene (i.e.F 0 animals injected with the NvDclk1::GFP plasmid) identified differences in the morphology of labelled cells in different parts of the animals.Cnidocytes around the mouth opening and at the tentacle tips possessed long stalks connecting the cell body to the base of the epithelium, with the stalk branching into several shorter processes at the base (Fig. 3E-G).Cnidocytes with more proximal positions in the tentacle (closer to the mouth) and cells in the body column extended several processes, but they lacked prominent stalks towards the base of the epithelium (Fig. 3E, H, I).Since NvDclk1 transcripts are enriched in NvElav1::mOrange + neurons, we next tested whether the NvDclk1::GFP transgene can be observed in these neurons.In double transgenic animals (with one allele of each transgene), GFP signal in the body column of planulae and primary polyps was weak, whereas the NvElav1::mOrange transgene labelled a large number of neurons and their neurites (Fig. 4A-C), as previously described [63].In older polyps, starting at around six weeks of age, the NvDclk1::GFP Taken together, the NvDclk1::GFP transgene labels cnidocytes that form an extensive network of neuritelike processes, and it is visible in a large part of the NvElav1::mOrange + neurons of juvenile polyps.

NvDclk1s localizes to microtubules in cnidocytes
Dcx-domain containing proteins have been shown to bind to microtubules, and microtubules support the development of the cnidocyst in Hydra and other cnidarians [70][71][72].To visualize the localization of microtubules in cnidocytes, we generated a transgene in which the regulatory elements of NvDclk1 drive the expression of the microtubule-binding domain of human ensconsin fused to three copies of GFP (NvDclk1::ensconsin-GFP [73]) .Injection of this construct labelled patches of cells in varying areas of the animals.In the tentacle tips, the GFP signal was prominent in filamentous structures at the apical end of cnidocytes and in the cnidocil, the sensory structure protruding from the cnidocytes into the exterior (Fig. 5A).In the body column, we found cells with labelling of a convoluted thread-like structure connected to an oval capsule with more prominent GFP signal on one side of the long axis of the capsule (Fig. 5B, C).The non-invaginated thread suggests that these cells are immature cnidocytes and the observations with the NvDclk1::ensconsin-GFP transgene are in line with descriptions of microtubules in cnidocytes based on electron microscopy and immunohistochemistry [70][71][72].To test whether NvDclk1 also localizes to microtubules in cnidocytes, we next generated a transgene in which a NvDclk1s-mCherry fusion protein is expressed under the control of the NvDclk1 regulatory elements (NvDclk1::Dclk1s-mCherry). We injected this construct together with the NvDclk1::ensconsin-GFP construct to observe potential colocalization.Though we did not recover double positive patches in the tentacle tips, cells in the body column showed near complete colocalization of the ensconsin-GFP and Dclk1s-mCherry signals (Fig. 5E-G).This suggests that NvDclk1 localizes to microtubules and might function as a microtubule binding protein, as described for vertebrate Dclk proteins.

NvDclk1 mutants lack mature cnidocytes
To analyze the function of NvDclk1 in cnidocyte development, we generated a mutant using the CRISPR/Cas9 system [74,75].The mutant has a 53 bp deletion located at the beginning of the first dcx domain.In the predicted protein resulting from this mutation, the first 14 amino acids of the first dcx domain are as in the wildtype allele, followed by 23 amino acids not found in the wildtype allele and a premature stop codon.The predicted protein is thus truncated before the middle of the first dcx domain and the mutation affects both splice variants (Additional Fig. 1A-C).
In crosses of heterozygous animals, we observed approximately 25% of primary polyps in which cnidocysts (the capsule inside the cnidocytes) were not visible in the tentacle tips (Fig. 6A, B) or the body cloumn (Fig. 6C, D) by light microscopy of living polyps.The cnidocyst phenotype in these animals was confirmed by a lack of signal from a modified DAPI staining protocol that labels the content of mature cnidocysts (Fig. 6E, F [76,77]).PCR confirmed that these animals represent homozygous mutants for NvDclk1 (Additional Fig. 1D).Histological staining of animals with this phenotype showed that a small number of cnidocyst-like structures were present in the tentacles, but they did not develop into the elongated capsules with an internalized thread that are observed in mature cnidocytes (Fig. 6G, H).Transmission electron microscopy revealed bent tentacle cnidocysts in the mutants that had not invaginated the thread (Fig. 6I, J) and often had an uneven surface of the capsule (Fig. 6K-M).
To analyze whether the nervous system is affected in NvDclk1 mutants, we crossed the mutant allele into the NvElav1::mOrange line and selected offspring carrying both the transgene and one mutant allele.Incrossing of these animals (NvDclk1 +/− , NvElav1::mOrange) resulted again in offspring that lacked cnidocysts in the tentacle tips, putatively homozygous for the mutant NvDclk1 allele.In contrast to the absence of mature cnidocytes, we could not detect defects in the NvElav1::mOrange + nervous system (Fig. 6E, F).We note, however, that subtle changes in the development or function of the nervous system would be difficult to detect with the available tools.
Taken together, the data show that NvDclk1 is required for the development of cnidocytes, a derived neural cell type specific to cnidarians.

Discussion
While many regulators of microtubules are present in all cell types of multicellular organisms, some regulate the cytoskeletal properties of only some cell types.Here we show that the microtubule-binding protein NvDclk1 is predominantly expressed in cells of the neural lineage in Nematostella, suggesting that the elaboration of neural morphology coincided with the acquisition of specific microtubule-regulating mechanisms during evolution.This is in line with a recent report in which comparative analyses of single cell RNA sequencing data suggested that genes related to neurite formation were gained in neural gene expression programs before the last common ancestor of cnidarians and bilaterians [78].This study, however, further found that additional genes related to the organization of microtubules were added to these gene expression programs in the lineage leading to bilaterians [78].Based on the previously described organization of microtubules during cnidocyte development, it is readily conceivable that perturbation of NvDclk1 function interferes with cnidocyst formation.The cnidocyst is a large post-Golgi structure that forms by addition of smaller vesicles to the growing capsule.It has a tubular extension at one end that becomes part of the thread that will be extruded upon activation of the mature cnidocyst.The thread invaginates into the lumen of the capsule where it is further modified.Maturation of the cnidocyst also involves stiffening of the capsule wall to allow the generation of osmotic pressure inside the capsule [79,80].Microtubules have been visualized as a cage-like structure at the thread-bearing pole of the growing capsule and around the forming thread [70][71][72].It has been proposed that they provide structural support for the growing thread and capsule, and they are potentially involved in the transport of vesicles from the Golgi to the capsule [70,71].Dclks and other dcx domain proteins have been shown to regulate the structure of the microtubule network and transport along microtubules [26,29,81].Our observation that NvDclk1 mutants contain cnidocysts with an irregular, bent shape and an uneven surface suggests that their maturation into elongated capsules with a smooth surface is perturbed.This is compatible with a role for NvDclk1 in the formation or maintenance of a microtubule structure that provides structural support for the cnidocyst.It remains to be determined whether this is based on a direct role in regulating microtubule properties, a function in regulating microtubule-based transport, or both.Other dcx domain-containing proteins have been shown to have analogous roles in regulating microtubule-based structural support of organelles, e.g. for the nucleus in migrating neurons [17,19] or for mechanosensory organelles in Drosophila mechanoreceptors [39,82].Though our data show that NvDclk1 is required for the differentiation of cnidocytes, we currently cannot rule out that it has an additional, earlier role in their specification.
We have here identified two splice variants of NvDclk1, with NvDclk1s lacking the C-terminal kinase domain.Similar splice variants have been recovered for Dclk genes in mice [83,84].The NvDclk1 mutant presented here truncates the protein in the first dcx domain.It thus does not distinguish between the long and short splice variants, and it therefore remains to be addressed whether the kinase domain is required for the function of NvDclk1 in cnidocyte development.
While our observations suggest a role for NvDclk1 in the regulation of microtubules, we currently cannot rule out that additional functions, e.g. in regulating the actin cytoskeleton [28,30,85], contribute to the phenotype of the NvDclk1 mutants.
The NvDclk1::GFP transgenic line revealed an elaborate network of cellular processes emerging from cnidocytes, as was also shown with a NvNematogalectin::EGFP transgene in a recent paper [68].It is tempting to speculate that these processes might represent neurites that allow communication among cnidocytes and between cnidocytes and other cells, e.g.neurons or secretory cells [86].This possibility is further supported by electron microscopy reconstructions of cnidocytes in Nematostella [69] and by earlier observations of synaptic contacts between sensory cells and cnidocytes in other cnidarians [87,88].If cnidocytes engage in local circuitry controlling their activity, it will be interesting to understand how such circuitry remains functional, given that cnidocytes are thought to be single-use cells that are lost after extrusion of the cnidocyst.
In contrast to the readily visible defect in cnidocyte development, we did not observe an effect of the NvD-clk1 mutation on the structure of the NvElav1::mOrangepositive nervous system.In the double transgenics, co-expression of NvDclk1::GFP and NvElav1::mOrange was not visible at planula stages.Though this in principle could explain the lack of a phenotype at primary polyp stage, we rather think that the lack of observable co-expression is due to low-level expression of a single allele of the NvDclk1::GFP transgene at these stages.This scenario is in line with the finding that only crosses of two NvDclk1::GFP heterozygotes yielded visible GFP expression in the body column of planulae.The lack of an apparent phenotype might instead be due to functional redundancy with other microtubule-binding proteins in neurons, but we also acknowledge that we currently do not have the tools to identify subtle effects on neural development or structure, e.g. in the timing of neurite outgrowth, the polarity of microtubules in neurites [89] or the formation of synapses.
Taken together we show here that NvDclk1 is predominantly expressed in cells of the Nematostella nervous system and that it is required for cnidocyte development.This supports the hypothesis that regulation of the microtubule cytoskeleton by dcx domain containing proteins is an ancient feature of nervous systems.

with primers G G T T T T C A G T C C A C C C G A T C A G (forward) and G G A T G A A A G A C A C T C C C A G T C (reverse).
NvDclk1l was amplified based on gene models Nve15812 and Nve15813 (https://figshare.com/articles/Nematostella_vectensis_transcriptome_ and_gene_models_v2_0/

807696) with primers A T G G A G A A T G G A A T G A T G A A T G G A G (forward) and G A C C C A G G G A T G T G C G A G C A C (reverse). Both splice variants
were cloned into pGEM-Teasy (Promega, US).

Transgenic reporter lines
The NvDclk1::GFP and NvDclk1::dclk1s-mCherry lines were generated by I-SceI-mediated transgenesis as described previously [91,92].For the NvDclk1 reporter line ca.2.9 kb upstream of the start codon were amplified and inserted via PacI and AscI sites in front of a GFP sequence with a C-terminal CAAX motif for membrane localization.The genomic coordinates for the regulatory region are 13,242,493-13,239,561 on the minus strand of chromosome 10 (https://simrbase.stowers.org/).For the NvDclk1::dclk1s-mCherry line, the ORF of NvDclk1s was inserted with AscI/AscI between the NvDclk1 promoter and the ORF for mCherry.For NvDclk1::ensconsin-GFP, the microtubule-binding domain of human ensconsin fused to three copies of EGFP [73] was amplified from Addgene plasmid #26,741 and inserted with PacI/AscI downstream of the NvDclk1 promoter.In all constructs, the cloning cassette was flanked by inverted I-SceI sites.Plasmids were digested with I-SceI for 30 min at 37ºC and injected at a concentration of 20 μg/μl [91,93].

Generation and genotyping of NvDclk1 mutants
The mutants were generated following the protocol described in [94].Single guide RNAs targeting the start of the first dcx domain were synthesized using primers

T A G G T T T C A A G C G A G C G C T A C A and A A A C T G T A G C G C T C G C T T G A A A.
Primers were annealed and inserted into vector pDR274 [94].sgRNAs were synthesized using the T7 MegaScript kit (Invitrogen, USA).500 ng/μl single guide RNA and 1.5 μg/μl nls-Cas9 (PNAbio, USA) were injected into fertilized eggs.Foot tissue of F1 animals was genotyped by amplifying and sequencing the region around the sgRNA target site with primers G C A

T C G G G A G A T A G A A T G G A (forward) and G A A G G T C G A T T T T C G C A G A C (reverse)
. Polyps heterozygous for a 53 bp deletion were crossed to obtain homozygous F2 and F3 mutants.The genotype of polyps lacking visible tentacle cnidocysts was determined by PCR with the same primers.

In situ hybridization and immunohistochemistry
Colorimetric and fluorescent in situ hybridization were done according to the protocols described in [59] and [61].The following protocol is edited from [61].
For fluorescence in situ hybridization, fixed samples were incubated in 2% hydrogen peroxide in methanol to quench endogenous hydrogen peroxidase activity.Samples were then rehydrated in PTW and the ISH protocol was followed from the Proteinase K incubation step until the end of the SSC/PTW RT washes.Samples were incubated with digoxigenin and fluorescein-labeled riboprobes (MEGAscript Kit, Invitrogen).After the SSC/ PTW RT washes, samples were washed in TNT (0.1 M Tris-HCl pH 7.5/0.15M NaCl/0.5% Triton X-100) and then blocked in TNTblock [0.5% blocking reagent (Perki-nElmer)/TNT] for 1 h at RT before overnight incubation with anti-digoxigenin (1:100) or anti-fluorescein (1:250) horseradish peroxidase (Roche).Unbound antibodies were removed by 10 15 min TNT washes, and samples were then incubated in fluorophore tyramide amplification reagent (TSA Plus Kit, Perkin Elmer).For double labeling, samples were washed in 0.1 M glycine pH 2.0 and incubated 1 h in TNT block before overnight incubation with anti-digoxygenin or anti-fluorescein horseradish peroxidase (Roche).Post-antibody washing and the TSA reaction were repeated as for the first probe; samples were then washed in TNT, incubated with DAPI 1:1000 and mounted in ProLong Gold antifade reagent.
Samples were imaged on either a Nikon Eclipse E800 compound microscope with a Nikon Digital Sight DSU3 camera, on a Leica SP5 or an Olympus FV3000 confocal microscope.

Histology and electron microscopy
For histology and electron microscopy, primary polyps were fixed in 2.5% glutaraldehyde/0.1 M cacodylate buffer (pH 7.2).Samples were transferred into 1.25% glutaraldehyde/0.1 M cacodylate buffer (pH 7.2) and stored at 4 °C until further processing.Polyps were then washed in 0.1 M cacodylate buffer and postfixed in 1% osmium tetroxide in the same buffer for 1 h.Samples were dehydrated through a graded series of ethanol and acetone and then embedded into Epon resine (SPI-Pon 812 Embedding Kit, Structure Probe Inc.) and sectioned using routine techniques by Leica ULTRACUT microtome.Semithin sections were stained in 1% solution of toluidine blue.Ultrathin sections were stained in 2% water solutions of uranyl acetate and in Reynolds' lead citrate solution [95] and examined by transmission electron microscopes JEOL JEM-1011 and JEOL JEM-1400.Sample processing was performed at the Michael Sars Centre (Bergen) and electron microscopy was performed at the Electron Microscopy Laboratory of the Shared Facilities Center of the Lomonosov Moscow State University.

Fig. 1
Fig. 1 NvDclk1 is expressed in scattered cells during development.(A) Schematic depictions of the domain composition of selected Nematostella (Nv) and human (Hs) dcx domain-containing proteins.The number of amino acids is indicated on the right side.(B-J) Lateral views of in situ hybridization with the oral pole oriented to the right.Probes are indicated on the left, developmental stages on top of the images.Note that for (B) the orientation is deduced from the expression in the endodermal plate at later stages.Scale bars: 50 μm

Fig. 2 A
Fig. 2 A NvDclk1::GFP reporter line labels a subset of NvDclk1-expressing cells.(A-F) Lateral views of double fluorescence in situ hybridizations, oral pole oriented to the right.Developmental stages are indicated on the left, probe on top.Not all NvDclk1-expressing cells also express the transgene-derived GFP mRNA.(G-K) Lateral views of NvDclk1::GFP transgenic animals at different developmental stages.GFP expression is detected by immunofluorescence with an anti-GFP antibody

Fig. 3
Fig. 3 NvDclk1::GFP labels cnidocytes and their processes.(A, B) Lateral views of NvDclk1::GFP transgenic animals (cyan) co-labelled with anti-NvNcol3 antibody (magenta) at gastrula (A) and planula (B) stages.B' and B'' are single channel images of higher magnifications of the area boxed in (B), with DNA labelled by DAPI (grey).Many NvDclk1::GFP-positive cells express NvNcol3.(C, D) Cnidocytes in the tentacles of NvDclk1::GFP (shown in cyan), NvNCol3::mOrange2 (magenta) double transgenic animals possess long processes.(E-I) NvDclk1::GFP-expressing cnidocytes in different body regions display different morphologies.Images are from animals injected with the NvDclk1::GFP plasmid.A minimum of five animals was analysed for each of the indicated body regions.Scale bars: 50 μm (A, B), 10 μm (C-I)

Fig. 4
Fig. 4 NvDclk1::GFP labels neurons in juvenile polyps.Confocal microscopy images of NvDclk1::GFP (in cyan), NvElav1::mOrange (in magenta) double transgenic animals.(A-C) Lateral views at tentacle bud stage, oral pole to the right.At this stage, co-expression of the two transgenes is not visible.(D-F) Views of the body column of 7 week-old polyps.Most NvElav1::mOrange-expressing neurons at this stage co-express NvDclk1::GFP.Two tracts of neurites along the base of the mesenteries running in an oblique orientation are visible.Scale bars: 50 μm (A-C), 20 μm (D-F)

Fig. 5
Fig. 5 NvDclk1s localizes to microtubules in cnidocytes.Confocal images of live primary polyps injected with NvDclk1::ensconsin-GFP only (A-C) or together with NvDclk1::Dclk1s-mCherry (E-G).The injection results in patches of cells expressing the transgenes.(A) Tentacle tip, (B, C) body column of NvDclk1::ensconsin-GFP expressing polyps.(C) is a higher magnification of the area boxed in (B), (D) is an interpretation of (C) with cnidocyst capsule and thread in brown and the GFP signal in green.(E-F) body column of a polyp injected with both transgenes show co-localization of the two signals.Scale bars 10 μm

Fig. 6
Fig. 6 NvDclk1 is required for cnidocyte differentiation.(A-D) DIC images of tentacle tips (A, B) and body colum (C, D) in the genotypes indicated in the upper right corner.Homozygous mutants lack the elongated cnidocysts that are found in the wildtype animals (arrows in A, C). (E, F) NvElav1::mOrange transgenics mutant for NvDclk1 lack mature cnidocysts, as shown by the absence of DAPI signal.The NvElav1::mOrange-positive nervous system does not show gross alterations in the mutants.Lateral views with oral end oriented to the right/upper right.(G, H) Semi thin sections of tentacles show elongated cnidocytes in wildtype (arrows in G) and fewer cnidocytes with bent cnidocysts in NvDclk1 mutants (arrow in H). n = 5 animals for wildtype, n = 16 animals for mutants.(I-M) Transmission electron microscopy of tentacle tips.In (I) cyan arrowheads indicate the cnidocyst of a mature, yellow arrowheads the capsule of an immature cnidocyte.The thread of the cnidocyst (yellow asterisks) is inside the mature cnidocyst, and partially outside the cnidocyst in the immature cnidocyst.In the inset in the upper right corner, yellow asterisks label invaginated parts of the thread.(J) TEM image of the cnidocyte in a NvDclk1 mutant.The cnidocyte capsule is bent and the thread has not been invaginated (multiple thread fragments are marked with the asterisks).(K) The capsule of immature wt cnidocyte, multiple thread fragments located near the capsule are marked with the asterisks.Note that the capsule wall is almost even.(L, M) The capsules of cnidocytes typical for NvDclk1 mutants; red lines follow parts of the uneven surface of the capsule walls.n = 3 animals for wild type, n = 5 animals for mutants.as -apical surface, n -cnidocyte nucleus.Scale bars 10 μm (A-D, G, H), 50 μm (E, F), 2 μm (I-K), 1 μm (L, M)